Nemluvio, which was also approved for prurigo nodularis, becomes Galderma’s first approved biologic in its dermatology ...
New EU regulations aim to speed up health technology assessments (HTAs), but the pharma industry raises logistical concerns.
CSL has received approval from the EC for Andembry (garadacimab) to prevent recurrent attacks of HAE in patients aged 12 ...
Newleos has closed an oversubscribed Series A financing round, raising $93.5m to revolutionise neuropsychiatric disorder ...
The Duchenne muscular dystrophy (DMD) landscape across the seven major markets (7MM) - the US, France, Germany, Italy, Spain, ...
Health Canada has approved Novartis Canada’s Fabhalta (iptacopan capsules) as the first oral monotherapy to treat adults with ...
US President Donald Trump kicked off his second term with a series of directives aimed at the US National Institutes of ...
Aardvark’s lead candidate ARD-101 is being investigated in a Phase III study for hyperphagia in Prader-Willi syndrome.
AbbVie has entered a partnership and option-to-license agreement with Xilio for tumour-activated, antibody-based ...
TriNetX has collaborated with Fujitsu to establish TriNetX Japan KK, a JV aimed at accelerating healthcare research and ...
With Dry January firmly behind us, many adults are prompted to reassess their relationship with alcohol. Alcohol Change, the ...
Wide areas of the pharmaceutical industry are ripe for enhancement, as examples from the industry’s top innovators reflect.
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